Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth 234962001

SNOMED CT code

SNOMED code

234962001

name

Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth

status

active

date introduced

2002-01-31

fully specified name(s)

Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth (disorder)

synonyms

Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth

attributes - group1

Pathological process

Pathological developmental process 308490002

Associated morphology

Morphologically abnormal structure 49755003

Finding site

Enamel structure 76993005

Occurrence

Congenital 255399007

parents

Amelogenesis imperfecta, hypoplastic type 109476006
Autosomal dominant hereditary disorder 11164009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Developmental disorder 5294002
Developmental hereditary disorder 363070008
Amelogenesis imperfecta 78494001
Amelogenesis imperfecta, hypoplastic type 109476006
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth 234962001

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Genetic disease 782964007
Hereditary disease 32895009
Autosomal hereditary disorder 1899006
Autosomal dominant hereditary disorder 11164009
Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth 234962001

ancestors

sorted most to least specific

Amelogenesis imperfecta, hypoplastic type 109476006
Autosomal dominant hereditary disorder 11164009
Amelogenesis imperfecta 78494001
Autosomal hereditary disorder 1899006
Hereditary disorder of tooth 1148766007
Developmental hereditary disorder 363070008
Congenital anomaly of tooth 422977003
Disorder of hard tissues of teeth 46557008
Congenital anomaly of digestive organ 128332003
Digestive system hereditary disorder 363080007
Congenital abnormality of oral cavity 282041002
Malformation of tooth 422775003
Congenital anomaly of jaw 95473006
Hereditary disorder by system 363137000
Disorder of tooth development 371136004
Congenital anomaly of mouth 128334002
Tooth disorder 234947003
Hereditary disease 32895009
Congenital anomaly of head 87290003
Congenital malformation of upper alimentary tract 275262008
Disorder of teeth AND/OR supporting structures 105995000
Genetic disease 782964007
Tooth finding 278544002
Disorder of digestive organ 76712006
Congenital anomaly of digestive tract 95470009
Oral cavity finding 116337000
Congenital anomaly of digestive system 69518005
Disease of mouth 118938008
Disorder of jaw 37156001
Finding of mouth region 423066003
Congenital malformation 276654001
Disorder of head 118934005
Disorder of upper digestive tract 50410009
Finding of head region 298364001
Developmental disorder 5294002
Congenital disease 66091009
Disorder of digestive tract 84410009
Head finding 406122000
Disorder of digestive system 53619000
Finding of head and neck region 118254002
Disorder of body system 362965005
Digestive system finding 386617003
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:

CPT® to SNOMED Crosswalks

Thank you for choosing Find-A-Code, please Sign In to remove ads.

MY NEWSLETTERS

FEES

FACILITY

RISK ADJUSTMENT

SNOMED CT Concept 138875005

Clinical finding 404684003

Disease 64572001

Developmental disorder 5294002

Developmental hereditary disorder 363070008

Amelogenesis imperfecta 78494001

Amelogenesis imperfecta, hypoplastic type 109476006

Amelogenesis imperfecta - hypoplastic autosomal dominant - smooth 234962001

SNOMED CT code